Iodide in Milk. Electrochemistry Discover the difference
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1 Application Note Food & Beverage The finest LC-EC Applications for Food & Beverage analysis Iodide Phenols Bisphenol A Catechins Flavonoids Phenols Antioxidants Resveratrol Epicatechin Quercetin Other polyphenols Carbohydrates Monosaccharides Lactose Other oligo- and polysaccharides Vitamins, minerals etc. A, C, D, E, and K Iodide Q10, ubiquinols n FlexCell with exchangeable working electrode n Diamond working electrode n Robust and reproducible analysis Summary In this application note a sensitive and reliable LC-EC method is presented for the analysis of iodide based on DC amperometry using a flow cell with a diamond working electrode. Conductive diamond has several advantages over conventional electrode materials such as a wide potential window in aqueous solutions, excellent chemical inertness and stability. ALEXYS Application Note # 212_004_03 Electrochemistry Discover the difference
2 Introduction Iodine is an essential trace element for humans. It is a component of the thyroid hormone thyroxin, which regulates the body s metabolic state and the growth and development in children. Iodine deficiency is an important health problem throughout much of the world. The dietary uptake of sufficient trace amounts of iodide is therefore necessary for mental and physical development. Important sources of iodide are seafood, diary products, iodized table salt and processed foods like iodized bread [1]. Table 1 LC-EC Conditions HPLC ALEXYS Iodide Analyzer (part no E) Flow rate 0.4 ml/min Flow cell FlexCell with MD WE and HyREF Temperature 35 C for separation and detection Range 2 μa/v ADF 0.5 Hz I-cell na HPLC in combination with electrochemical detection is commonly used for the analysis of iodide in urine [2,3] and food products [4,5]. 2 na Iodide Figure 1: ALEXYS Iodide Analyzer Time [min.] Figure 2: Chromatogram of a 400 nm of potassium iodide (KI) in water (50.8 μg/l Iodide).Injection volume 20 μl. Method The ALEXYS Iodide analyzer is equipped with a DECADE Elite electrochemical detector and FlexCell with replaceable diamond electrode disc. The LC conditions used with the ALEXYS Iodide Analyzer were selected with the focus on the analysis of iodide in dairy products. Therefore, the same mobile phase and similar separation conditions were used as described in literature [4,5]. 2
3 Results A hydrodynamic voltammogram was recorded in the potential range between 900 and 2400 mv (vs. HyREF) to determine the optimum detection potential, using a 10 μm KI solution in water. Although the onset of the limiting current was observed at 2000 mv, a lower potential of 1500 mv was chosen for detection. At this potential a low background current (<30 na) and noise level are attained in combination with a good detection sensitivity for Iodide. In Figure 2 an example chromatogram is shown of 50.8 μg/l potassium iodide in water (injection volume 20 μl). The peak efficiency for the iodide peak was theoretical plates/meter. Linearity and detection limits Calibration curves were recorded with Iodide standards in the concentration range between 6 μg/l 1.3 mg/l. Within this concentration range a linear detector response was observed with correlation coefficients better than Iodide Area ( μa.s) Iodide concentration (mg/l) 5 na Figure 4: Calibration plot for Iodide in water. Concentration range 6 μg/l 1.3 mg/l. R = Iodide Time [min.] Figure 3: Chromatogram of Iodide in low-fat (1.5%) milk sample. Injection volume 20 μl. 3
4 A concentration detection limit (clod) of approximately 0.4 μg/l (3 nm) was found, demonstrating the excellent detection sensitivity achieved with the MD electrode. The clod is based on an injection volume of 20 μl and defined as the concentration that gives a signal that is three times the peakto-peak noise. Repeatability The repeatability of the method was evaluated by executing 10 repetitive injections (20 μl injection volume) of a 0.13 mg/l and 1.23 mg/l iodide solution. The relative standard deviation (RSD%) for retention time, peak area and height are listed in Table 2 for both concentrations. The relative standard deviation for both peak height and peak area are 1% or better at a concentration of 0.13 mg/l and % at 1.26 mg/l. The long-term repeatability was assessed with a standard with a high iodide concentration of 13.7 mg/l. 225 repetitive injections were performed in a time period of 22 hours, see Figure 5. For this experiment the flow rate was increased with a factor 2 (0.8 ml/min, system backpressure approximately 180 bar) to reduce the analysis time (6 minutes). After the 20 th injection a gap of 6 injections is visible due to an empty vial. 50 Table 2 Repeatability (n=10) Iodide (mg/l) tr Area Height Iodide Area ( A.s) Number of injections Figure 5: Long-term repeatability of DC amperometric detection of iodide on an MD electrode. Sample concentration 13.7 mg/l, injection volume 20 μl. The relative standard deviations (RSD%) for the peak area was 1.4%. It demonstrates the good response stability of MD, even at high iodide concentration. It has been observed that online electrochemical regeneration/ activation is an effective method to restore the detection sensitivity in case the response of the Magic Diamond electrode attenuated over time, or the electrode has not been used for a while. The flow cell does not have to be disassembled in this case. During the online regeneration procedure the detector was operated in the SCAN mode. Typically, the electrode was scanned between 3 Volts and + 3 Volts in mobile phase, with a scan rate of 50 mv/s.. 4
5 Iodide in milk products In Figure 3 an example chromatogram of a low-fat (1.5%) milk sample is shown. The following sample preparation procedure was performed prior to injection n 1 ml 3% acetic acid was mixed with 5 ml of sample for deproteination of the milk solution. The acidified solution was centrifuged and the supernatant collected. n Subsequently, the supernatant was passed over a RP SPE column (Alltech C18-fast column) for further clean-up of the milk matrix (removal of fat). n The eluate (first 2 ml discarded) was collected and 20 ul injected in the LC system. It should be stated that the sample preparation procedure described above is not validated and is only used to obtain a series of example chromatograms. The iodide peak in the chromatogram was identified by spiking a second milk sample prior to sample work-up with a known amount of Iodide, corresponding to a concentration of 317 μg/l. It is evident from Figure 3 that the iodide peak is well separated from the matrix. The concentration of iodide in the milk sample was estimated to be 45 μg/l. Conclusion The ALEXYS Iodide Analyzer provides a user-friendly and reliable solution for the determination of iodide by means of DC amperometry. With the new inert Magic Diamond electrode, iodide can be detected with excellent reproducibility and sensitivity. 5
6 References 1. John T. Dunn, Editorial: What s happening to our Iodine?, J Clin Endocrinol Metab., 83(10), 1998, K.Han, W. Koch, K.W. Pratt, Improved procedure for the determination of Iodide by Ion Chromatography with Electrochemical detection, Anal. Chem., 59, 1987, J. Rendl, S. Seybold, W. Borner, Urinary Iodide determined by Paired-Ion Reversed Phase HPLC with Electrochemical de-tection, Clin. Chem., 40/6, 1994, Determination of iodide content in milk and dried milk by HPLC, International IDF standard, 167: Milk and dried milk Determination of iodide contents method using HPLC, International ISO standard, 14378: W.R. LaCourse, Pulsed Electrochemical Detection in High Performance Liquid Chromatography, John Wiley & Sons, New York, 1 ed, Alexander Kraft, Doped diamond: A compact review on a new, versatile electrode material, Int. J. Electrochem. Sci., 2, 2007, Ordering information E ALEXYS Iodide Analyzer ALE-315 column, 150x3.0mm, 3um C18 Antec Scientific (USA) info@antecscientific.com T Antec Scientific (worldwide) info@antecscientific.com T For research purpose only. The information shown in this communication is solely to demonstrate the applicability of the ALEXYS system. The actual performance may be affected by factors beyond Antec s control. Specifications mentioned in this application note are subject to change without further notice. 6
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